Sui Shiyuan, Wu Hao, Guo Yuanyuan, Chen Gongming, Chang Junbiao, Bai Dachang
State Key Laboratory of Antiviral Drugs, NMPA Key Laboratory for Research and Evaluation of Innovative Drug, School of Chemistry and Chemical Engineering, Pingyuan Laboratory, Henan Normal University, Xinxiang, 453007, China.
Angew Chem Int Ed Engl. 2025 Sep 8;64(37):e202509640. doi: 10.1002/anie.202509640. Epub 2025 Jul 30.
ε-Lactams are important structural motifs in medicinal chemistry, but a fully enantioselective synthesis without byproduct formation represents a challenge that has attracted significant research interest. Herein, we report an atom- and step-economic synthesis of chiral ε-lactams via Rh(I)-catalyzed enantioselective C─C bond activation of aminocyclopropanes. The catalytic C─C bond activation enables a directed generation of chiral rhodacyclobutanes that circumvents β-hydride decomposition. Subsequent enantioselective cycloaddition of the alkene unit and then fragmentation generates chiral ε-lactams. A range of enantioenriched ε-lactams have been obtained with excellent regio- and enantioselectivities, which can undergo several stereospecific transformations. Theoretical calculations are performed to reveal the reaction mechanism and the origin of enantioselectivity control.
ε-内酰胺是药物化学中的重要结构单元,但无副产物生成的完全对映选择性合成是一项具有挑战性的任务,已引起了广泛的研究兴趣。在此,我们报道了通过铑(I)催化的氨基环丙烷对映选择性C─C键活化实现手性ε-内酰胺的原子和步骤经济性合成。催化C─C键活化能够直接生成手性铑环丁烷,从而避免β-氢化物分解。随后烯烃单元的对映选择性环加成以及碎片化反应生成手性ε-内酰胺。已获得了一系列具有优异区域和对映选择性的对映体富集ε-内酰胺,它们可进行多种立体特异性转化。进行了理论计算以揭示反应机理和对映选择性控制的起源。